A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561371



Internal ID20934442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12000165..12359085hg38UCSC Ensembl
chr9:12000165..12359085hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38358921
hg19358921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561371
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer